rac-(1R,4R,6R)-2-oxabicyclo[2.2.1]heptan-6-ol

Base Information

Chemical Name:rac-(1R,4R,6R)-2-oxabicyclo[2.2.1]heptan-6-ol
CAS No.:36368-46-4
Molecular Formula:C6H10O2
Molecular Weight:114.144
Hs Code.:
European Community (EC) Number:891-447-8

Synonyms:SCHEMBL10774161;EN300-28316189;rac-(1R,4R,6R)-2-oxabicyclo[2.2.1]heptan-6-ol;36368-46-4

Suppliers and Price of rac-(1R,4R,6R)-2-oxabicyclo[2.2.1]heptan-6-ol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of rac-(1R,4R,6R)-2-oxabicyclo[2.2.1]heptan-6-ol

Chemical Property:

XLogP3:0
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:114.068079557
Heavy Atom Count:8
Complexity:103

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C2CC(C1O)OC2
Isomeric SMILES:C1[C@@H]2C[C@H]([C@@H]1O)OC2

Technology Process of rac-(1R,4R,6R)-2-oxabicyclo[2.2.1]heptan-6-ol

There total 1 articles about rac-(1R,4R,6R)-2-oxabicyclo[2.2.1]heptan-6-ol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 25125-21-7
4-(hydroxymethyl)cyclopentene

: 36368-46-4
exo-2-Oxabicyclo<2.2.1>heptan-6-ol

Guidance literature:: Multi-step reaction with 2 steps

1: m-chloroperbenzoic acid (85percent) / CH₂Cl₂ / 1.) 0 deg C, 1 h, 2.) room temperature, 3 h

2: 40 percent / 0.42 N butyllithium / diethyl ether; tetrahydrofuran / 69 h / Heating

With n-butyllithium; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/jo00330a027